A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519475



Internal ID15446768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133029797..133153534hg38UCSC Ensembl
Innerchr6:133350936..133474673hg19UCSC Ensembl
Innerchr6:133392629..133516366hg18UCSC Ensembl
Innerchr6:133392629..133516366hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38123738
hg19123738
hg18123738
hg17123738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656310, nssv681290
Samples
Known GenesLINC00326
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519475
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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